| Title : Enantioselective esterification of racemic ibuprofen in isooctane by immobilized lipase on cellulose acetate-titanium iso-propoxide gel fiber - Ikeda_2002_J.Biosci.Bioeng_93_98 |
| Author(s) : Ikeda Y , Kurokawa Y |
| Ref : J Biosci Bioeng , 93 :98 , 2002 |
|
Abstract :
Lipase (Candida rugosa) was entrap-immobilized on cellulose acetate-titanium iso-propoxide gel fiber by the sol-gel method. The immobilized lipase was used for the direct synthesis of (S)-ibuprofen ester from racemic ibuprofen using propyl alcohol as an acyl acceptor in isooctane. The activity of the immobilized lipase was decreased to about 10-20% that of native lipase. However, the reaction was more enantioselective compared to that with native lipase. The stability for repeated use was improved by immobilization. |
| PubMedSearch : Ikeda_2002_J.Biosci.Bioeng_93_98 |
| PubMedID: 16233173 |
Ikeda Y, Kurokawa Y (2002)
Enantioselective esterification of racemic ibuprofen in isooctane by immobilized lipase on cellulose acetate-titanium iso-propoxide gel fiber
J Biosci Bioeng
93 :98
Ikeda Y, Kurokawa Y (2002)
J Biosci Bioeng
93 :98